Purity Farmapiel Hand Sanitizer 70% Alcohol

Manufacturer
Centro Internacional de Cosmiatría S.A.P.I. de C.V.
Effective date
2020-08-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:18:11

Label at a glance#

ProductPurity Farmapiel Hand Sanitizer 70% Alcohol
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

To decrease bacteria on the skin when water, soap & towel are not available - Recommended for repeated use.

Dosage and administration

Apply enough product to wet hands. Rub hands together until dry. Supervise children in use of this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin when water, soap & towel are not available - Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable - Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, rinse thoroughly with water. Do not use on broken or irritated skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or redness develop and last more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply enough product to wet hands. Rub hands together until dry. Supervise children in use of this product.

Other information

OTHER SAFETY INFORMATION

  • Do not store above 105°F (40°C)
  • May discolor certain wood surfaces

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

water, glycerin, aloe barbadensis leaf juice, carbomer, triethanolamine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59.14 mL Label59.14 mL Label59.14 mL (2oz) NDC: 77229-002-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118.29 ml 4Oz118.29 ml 4Oz118.29mL (4oz) NDC 77229-002-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236.58mL (8 oz) NDC: 77229-002-03

236.58 mL 8Oz236.58 mL 8Oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

473.17 mL 16Oz473.17 mL 16Oz473.17mL (16oz) NDC: 77229-002-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

946.35mL 32Oz946.35mL 32Oz946.35mL (32oz) NDC: 77229-002-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 2Oz TubeLabel 2Oz Tube59.14mL 2Oz NDC 77229-002-06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77229-00277229-002-01, 77229-002-02, 77229-002-03, 77229-002-04, 77229-002-05, 77229-002-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c74261a0-62da-5226-e053-2995a90a9275a8d7486c-cd2d-249e-e053-2995a90a3a5d2021-07-16WarningsExact identifier
spl set id: a8d7486c-cd2d-249e-e053-2995a90a3a5d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.